Canonical Allele Identifier: CA2648792155
Gene: FCGR2C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161589993_161589994insGAAAAA , CM000663.2:g.161589993_161589994insGAAAAA GRCh38
NC_000001.10:g.161559783_161559784insGAAAAA , CM000663.1:g.161559783_161559784insGAAAAA GRCh37
NC_000001.9:g.159826407_159826408insGAAAAA NCBI36
NG_011982.1:g.13655_13656insGAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000699402.1:c.41-40963_41-40962insTTTTTC ENSP00000514363.1:n.41-40963_41-40962insTTTTTC
ENST00000699403.1:c.61+40374_61+40375insTTTTTC ENSP00000514364.1:n.61+40374_61+40375insTTTTTC
ENST00000465075.6:n.484-88_484-87insGAAAAA
ENST00000466542.6:c.391+174_391+175insGAAAAA ENSP00000426627.1:n.391+174_391+175insGAAAAA
ENST00000473530.6:n.572+174_572+175insGAAAAA
ENST00000473712.6:n.413+174_413+175insGAAAAA
ENST00000482226.2:n.370+174_370+175insGAAAAA
ENST00000543859.5:c.388+174_388+175insGAAAAA ENSP00000444663.2:n.388+174_388+175insGAAAAA
ENST00000611236.1:c.388+174_388+175insGAAAAA ENSP00000480953.1:n.388+174_388+175insGAAAAA
NR_047648.1:n.490+174_490+175insGAAAAA